MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
Medtronic MiniMed, Inc.
The hazard
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA). FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI-DI/GTIN: A7630006392701Model 00763000521554Model 00763000639273Model A7630006392301Model 00199150035687Model A7630007325603Model A7630007325601Model 00763000639235Model A7630007325604Model 00763000384289Model 00763000521530Model A7630007325401Model 00763000521547Model A7630006392601Model A7630006392201Model 00763000639228Model 00199150035663Model 00763000639266Model A7630007325404Model 00199150035694Model 00763000442194Model A7630007325403Model 00763000521523. Software version 6.62UPC 00763000521554UPC 00763000639273UPC 00199150035687UPC 00763000639235UPC 00763000384289UPC 00763000521530UPC 00763000521547UPC 00763000639228UPC 00199150035663UPC 00763000639266UPC 00199150035694UPC 00763000442194UPC 00763000521523Would you have heard about this one?
RapidRecall watches everything you own against every new federal recall and emails you the moment something you bought turns up. Free for your most important items.
Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.